Federica Zibordi

Fondazione IRCCS Istituto Neurologico "C. Besta"

Emailzibordi.f@istituto-besta.it

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53 Article
3 Review article

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study
Groeneweg, S., van Geest, F. S., Abacı, A., Alcantud, A., Ambegaonkar, G. P., Armour, C. M., Bakhtiani, P., Barca, D., Bertini, E. S., van Beynum, I. M., Brunetti-Pierri, N., Bugiani, M., Cappa, M., Cappuccio, G., Castellotti, B., Castiglioni, C., Chatterjee, K., de Coo, I. F. M., Coutant, R., Craiu, D. & 30 others, Crock, P., DeGoede, C., Demir, K., Dica, A., Dimitri, P., Dolcetta-Capuzzo, A., Dremmen, M. H. G., Dubey, R., Enderli, A., Fairchild, J., Gallichan, J., George, B., Gevers, E. F., Hackenberg, A., Halász, Z., Heinrich, B., Huynh, T., Kłosowska, A., van der Knaap, M. S., van der Knoop, M. M., Konrad, D., Koolen, D. A., Krude, H., Lawson-Yuen, A., Lebl, J., Linder-Lucht, M., Paone, L., Spada, M., Tonduti, D. & Zibordi, F., Jul 2020, In: The Lancet Diabetes and Endocrinology. 8, 7, p. 594-605 12 p.
Research output: Contribution to journal › Article › peer-review
Vascular Remodeling in Moyamoya Angiopathy: From Peripheral Blood Mononuclear Cells to Endothelial Cells
Tinelli, F., Nava, S., Arioli, F., Bedini, G., Scelzo, E., Lisini, D., Faragò, G., Gioppo, A., Ciceri, E. F., Acerbi, F., Ferroli, P., Vetrano, I. G., Esposito, S., Saletti, V., Pantaleoni, C., Zibordi, F., Nardocci, N., Zedde, M. L., Pezzini, A., Di Lazzaro, V. & 7 others, Capone, F., Dell'Acqua, M. L., Vajkoczy, P., Tournier-Lasserve, E., Parati, E. A., Bersano, A. & Gatti, L., Aug 11 2020, In: International Journal of Molecular Sciences. 21, 16
Research output: Contribution to journal › Article › peer-review
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial
Groeneweg, S., Peeters, R. P., Moran, C., Stoupa, A., Auriol, F., Tonduti, D., Dica, A., Paone, L., Rozenkova, K., Malikova, J., van der Walt, A., de Coo, I. F. M., McGowan, A., Lyons, G., Aarsen, F. K., Barca, D., van Beynum, I. M., van der Knoop, M. M., Jansen, J., Manshande, M. & 26 others, Lunsing, R. J., Nowak, S., den Uil, C. A., Zillikens, M. C., Visser, F. E., Vrijmoeth, P., de Wit, M. C. Y., Wolf, N. I., Zandstra, A., Ambegaonkar, G., Singh, Y., de Rijke, Y. B., Medici, M., Bertini, E. S., Depoorter, S., Lebl, J., Cappa, M., De Meirleir, L., Krude, H., Craiu, D., Zibordi, F., Oliver Petit, I., Polak, M., Chatterjee, K., Visser, T. J. & Visser, W. E., Sep 2019, In: The Lancet Diabetes and Endocrinology. 7, 9, p. 695-706 12 p.
Research output: Contribution to journal › Article › peer-review
Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study
Carecchio, M., Invernizzi, F., Gonzàlez-Latapi, P., Panteghini, C., Zorzi, G., Romito, L., Leuzzi, V., Galosi, S., Reale, C., Zibordi, F., Joseph, A. P., Topf, M., Piano, C., Bentivoglio, A. R., Girotti, F., Morana, P., Morana, B., Kurian, M. A., Garavaglia, B., Mencacci, N. E. & 2 others, Lubbe, S. J. & Nardocci, N., Oct 1 2019, In: Movement Disorders. 34, 10, p. 1516-1527 12 p.
Research output: Contribution to journal › Article › peer-review
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease—study protocol and preliminary results
on behalf of GEN-O-MA study group, Jan 1 2019, (Accepted/In press) In: Neurological Sciences.
Research output: Contribution to journal › Article › peer-review

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

Vascular Remodeling in Moyamoya Angiopathy: From Peripheral Blood Mononuclear Cells to Endothelial Cells

Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial

Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study

GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease—study protocol and preliminary results